Canonical Allele Identifier: CA84451147
Gene: MRPS22 HGNC NCBI

Linked Data

dbSNP Id: rs11706018

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139197551C>T , CM000665.2:g.139197551C>T GRCh38
NC_000003.11:g.138916393C>T , CM000665.1:g.138916393C>T GRCh37
NC_000003.10:g.140399083C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000495075.5:c.-72+17191C>T ENSP00000418008.1:n.-72+17191C>T
ENST00000495225.1:c.82+34341C>T ENSP00000417104.1:n.82+34341C>T